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绥美凯最佳服药时间

Author: Medicalhalo
Release time: 2025-10-19 11:44:20

(Dolutea Balami Tablets) has been approved by the State Food and Drug Administration for official marketing in China. It not only has the characteristics of good tolerability, high resistance barrier, and small drug interactions, but also has the advantage of being convenient to take. By taking one tablet a day and one tablet at a time, the medication burden of AIDS patients can be reduced to a certain extent, thereby improving the patient's medication compliance and significantly improving the patient's quality of life. So, when is the best time to take Suimeikai?

There is no specific requirement for the taking time of Suimeikan (Dolutea Abalamib Tablets). For adults and adolescents, the recommended dosage of Suimeike (Dolutea Abalamib Tablets) is one tablet each time, once a day. It is best to take it at the same time every day to ensure the continuous effect of the medicine. Adults or adolescents whose body weight is less than 40 kg should not be given this product because Trimax is a fixed-dose tablet and the dose cannot be reduced.

There are limited data on the use of dolutegravir, abacavir, and lamivudine in patients aged ≥65 years, and there is no evidence that older patients require different doses than younger adults. Taking into account age-related changes, such as decreased renal function and changes in hematological parameters, special caution is recommended when administering the drug in this age group.

Clinical data on dolutegravir are limited, and the most commonly reported adverse reactions that may or may be related to dolutegravir and abacalongvir/lamivudine (pooled data from 679 antiretroviral-naïve subjects who received this combination in Phase IIb to IIb clinical trials) are nausea (12%), insomnia (7%), dizziness (6%), and headache (6%). Many adverse reactions (nausea, vomiting, diarrhea, fever, drowsiness, rash) occur frequently in patients with abacavir hypersensitivity. Therefore, patients who develop these symptoms should be carefully evaluated for the presence of this hypersensitivity reaction.

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